Anatomy Supply Partners recalls SAFE-T-FILL Micro Collection Tube Extenders (Model 09 1004) due to inadequate quality control during manufacturing. Affected units were produced from August 2020 to February 2025.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling SAFE-T-FILL Micro Collection Tube Extenders (Model 09 1004) because they were made using unvalidated manufacturing processes. This could lead to product failure, but the recall does not specify immediate safety risks.
The product was manufactured under an inadequate quality system, meaning unvalidated manufacturing processes were used. This could result in product failure, but the recall does not specify how this affects safety during normal use.
Healthcare professionals and lab users who own or use the SAFE-T-FILL Micro Collection Tube Extenders (Model 09 1004) are affected. Those most at risk are users who have the specific model numbers produced between August 2020 and February 2025.
Check for the model number 09 1004 on the product. The affected units were produced from August 2020 to February 2025 with specific lot numbers: 21D4585, 22E4059, 22J4037, 23I4016, 23J4029.
Identify the model number and production dates to confirm if your unit is affected.
The recall states the product was made with unvalidated manufacturing processes, but it does not specify immediate safety risks. The hazard is described as a quality issue, not a direct safety hazard.
The recall does not provide a remedy, so no action is required beyond checking if your product is affected.
Affected lot numbers are 21D4585, 22E4059, 22J4037, 23I4016, and 23J4029, produced between August 2020 and February 2025.
We’ve drafted a message you can send Anatomy Supply Partners to request your refund or repair — edit it as you like.
Subject: Recall Z-0567-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0567-2026 from Anatomy Supply Partners. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
